Detalhe da pesquisa
1.
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale.
Ann Neurol
; 89(5): 967-978, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576057
2.
Comparison of strength testing modalities in dysferlinopathy.
Muscle Nerve
; 66(2): 159-166, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35506767
3.
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal study.
Muscle Nerve
; 65(5): 531-540, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35179231
4.
Performance of Upper Limb module for Duchenne muscular dystrophy.
Dev Med Child Neurol
; 62(5): 633-639, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31538331
5.
Factors Associated With Early Motor Function Trajectories in DMD After Glucocorticoid Initiation: Post Hoc Analysis of the FOR-DMD Trial.
Neurology
; 102(10): e209206, 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710006
6.
Detecting meaningful change using the North Star Ambulatory Assessment in Duchenne muscular dystrophy.
Dev Med Child Neurol
; 55(11): 1046-52, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23909763
7.
Novel approaches to analysis of the North Star Ambulatory Assessment (NSAA) in Duchenne muscular dystrophy (DMD): Observations from a phase 2 trial.
PLoS One
; 17(8): e0272858, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35998119
8.
Validation of the North Star Assessment for Limb-Girdle Type Muscular Dystrophies.
Phys Ther
; 102(10)2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35932452
9.
Functional outcome measures in young, steroid-naïve boys with Duchenne muscular dystrophy.
Neuromuscul Disord
; 32(6): 460-467, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35618576
10.
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach.
Front Neurol
; 13: 828525, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35359643
11.
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease.
Neuromuscul Disord
; 31(4): 265-280, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33610434
12.
Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort Study.
Neurology
; 96(4): e587-e599, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33067401
13.
Assessment of disease progression in dysferlinopathy: A 1-year cohort study.
Neurology
; 2019 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30626655
14.
Editorial: Lessons Learned from Translational Research in Neuromuscular Diseases: Impact on Study Design, Outcome Measures and Managing Expectation.
Front Genet
; 13: 840074, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35860463